Direct and semi-direct resin composite restoration in large cavity preparations: analysis of dentin bond strength stability and bottom/top microhardness ratio in a cavity model.

To evaluate the influence of the restorative approach and aging time on dentin bond strength (BS), failure mode (FM), and bottom/top microhardness ratio (B/T) in a large dentin cavity model. A total of 102 bovine incisors were used to produce models of conical dentin cavities (4.0 mm thickness × 4.8 mm top diameter × 2.8 mm bottom diameter), which were restored using semi-direct filling (SDF) (Filtek™ Z250 XT + Scotchbond™ Universal/RelyX™ Ultimate luting system), direct bulk filling (DBF) (Filtek™ One Bulk Fill), and direct incremental filling (DIF) (Filtek™ Z250 XT) techniques. B/T, BS, and FM (n = 17) were analyzed in a microhardness tester, a universal testing machine, and a stereomicroscope, respectively, after 24 h and 6 months of water storage. BS and B/T data were analyzed using two-way ANOVA/Tukey post-hoc test (p < 0.05), while FM data were analyzed descriptively. There was a statistically significant difference in BS between the restorative techniques, and BS was influenced by aging time in the DBF and SDF groups. Mixed failure was predominant for the SDF technique in both aging times. There was no statistically significant difference in B/T among the restorative approaches regardless of the aging time (p > 0.05). Although all restorative approaches provided similar B/T, the semi-direct technique showed better performance on the material bond strength to dentine in large cavities.

In-office tooth bleaching with 38% hydrogen peroxide promotes moderate/severe pulp inflammation and production of ll-1ß, TNF-ß, GPX, FGF-2 and osteocalcin in rats.

OBJECTIVES: To study the intensity of inflammatory infiltrate and production of interleukin-1ß (ll-1ß), tumor necrosis factor-ß (TNF-ß), fibroblast growth factor-2 (FGF-2), glutathione peroxidase (GPX), and osteocalcin in response to in-office tooth bleaching in rats. MATERIAL AND METHODS: Twenty male Wistar rats were randomized into four groups (n=5) according to the received treatment (tooth bleaching or no treatment - control) and the period of euthanasia after treatment (24 h or 10 days). We performed tooth bleaching using a 38% hydrogen peroxide gel on maxillary and mandibular incisors. After euthanasia, incisors (20 per group) were processed for histological analysis, immunohistochemistry staining of ll-1ß, TNF-ß, FGF-2 and GPX and osteocalcin by immunofluorescence. We analyzed data using the Mann-Whitney and Kruskal-Wallis/Dunn tests (p<0.05). RESULTS: The bleached groups presented statistically significant differences regarding the pulp inflammation stage compared with the control groups. Bleached teeth showed moderate/severe inflammatory infiltrate and control groups presented absent inflammatory cells or a negligible number of mononuclear cells (p<0.001) at two times (24 h and 10 days). There was strong staining for ll-1ß, TNF-ß, and GPX in bleached groups at 24 h and strong staining for ll-1ß, TNF-ß, GPX and FGF-2 at 10 days. After 10 days of tooth bleaching, the bleached group showed a statistically superior amount of osteocalcin than the other groups (p<0.01). CONCLUSIONS: Tooth bleaching with 38% hydrogen peroxide causes severe pulp inflammation, but characteristics of tissue repair after 10 days.